TW200914579A - Aromatic amine derivative and organic electroluminescent element using the same - Google Patents

Aromatic amine derivative and organic electroluminescent element using the same Download PDF

Info

Publication number: TW200914579A
Authority: TW; Taiwan
Prior art keywords: group; carbon number; substituted; unsubstituted; ring
Prior art date: 2007-06-18

Application number

TW097122736A

Other languages

English (en)

Chinese (zh)

Inventor

Masakazu Funahashi

Shintaro Iwamoto

Mitsunori Ito

Yumiko Mizuki

Original Assignee

Idemitsu Kosan Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2007-06-18

Filing date

2008-06-18

Publication date

2009-04-01

2008-06-18 Application filed by Idemitsu Kosan Co filed Critical Idemitsu Kosan Co

2009-04-01 Publication of TW200914579A publication Critical patent/TW200914579A/zh

Links

150000004982 aromatic amines Chemical class 0.000 title claims abstract description 58
239000000463 material Substances 0.000 claims abstract description 74
239000010409 thin film Substances 0.000 claims abstract description 8
239000002904 solvent Substances 0.000 claims abstract description 7
229910052799 carbon Inorganic materials 0.000 claims description 396
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 348
-1 sulphur amine Chemical class 0.000 claims description 193
125000003118 aryl group Chemical group 0.000 claims description 184
230000015572 biosynthetic process Effects 0.000 claims description 95
125000000217 alkyl group Chemical group 0.000 claims description 72
150000001721 carbon Chemical class 0.000 claims description 62
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 61
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 45
125000004432 carbon atom Chemical group C* 0.000 claims description 40
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 32
125000001424 substituent group Chemical group 0.000 claims description 29
150000001875 compounds Chemical class 0.000 claims description 26
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 26
125000001624 naphthyl group Chemical group 0.000 claims description 25
125000000623 heterocyclic group Chemical group 0.000 claims description 23
239000010408 film Substances 0.000 claims description 19
125000000753 cycloalkyl group Chemical group 0.000 claims description 18
239000000126 substance Substances 0.000 claims description 18
229910052786 argon Inorganic materials 0.000 claims description 16
125000004429 atom Chemical group 0.000 claims description 16
239000002689 soil Substances 0.000 claims description 16
125000003396 thiol group Chemical group [H]S* 0.000 claims description 15
KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical group [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 13
150000001412 amines Chemical class 0.000 claims description 13
NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 claims description 13
150000002923 oximes Chemical class 0.000 claims description 10
125000003545 alkoxy group Chemical group 0.000 claims description 9
229910052801 chlorine Inorganic materials 0.000 claims description 8
125000002947 alkylene group Chemical group 0.000 claims description 7
125000001309 chloro group Chemical group Cl* 0.000 claims description 7
125000001072 heteroaryl group Chemical group 0.000 claims description 7
229920006395 saturated elastomer Polymers 0.000 claims description 7
125000005110 aryl thio group Chemical group 0.000 claims description 6
239000004575 stone Substances 0.000 claims description 6
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
150000001335 aliphatic alkanes Chemical class 0.000 claims description 5
125000004093 cyano group Chemical group *C#N 0.000 claims description 5
239000002019 doping agent Substances 0.000 claims description 5
239000007789 gas Substances 0.000 claims description 5
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
239000005864 Sulphur Substances 0.000 claims description 4
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 4
125000003710 aryl alkyl group Chemical group 0.000 claims description 4
239000003610 charcoal Substances 0.000 claims description 4
239000000203 mixture Substances 0.000 claims description 3
238000006467 substitution reaction Methods 0.000 claims description 3
125000000468 ketone group Chemical group 0.000 claims description 2
125000003107 substituted aryl group Chemical group 0.000 claims 3
230000005284 excitation Effects 0.000 claims 2
NBJKWEHXLWUBOS-UHFFFAOYSA-N 14h-phenanthro[9,10-b]chromene Chemical class C12=CC=CC=C2C2=CC=CC=C2C2=C1CC1=CC=CC=C1O2 NBJKWEHXLWUBOS-UHFFFAOYSA-N 0.000 claims 1
206010012239 Delusion Diseases 0.000 claims 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims 1
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 1
229910052787 antimony Inorganic materials 0.000 claims 1
WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims 1
231100000868 delusion Toxicity 0.000 claims 1
238000010586 diagram Methods 0.000 claims 1
238000005401 electroluminescence Methods 0.000 claims 1
239000001257 hydrogen Substances 0.000 claims 1
229910052739 hydrogen Inorganic materials 0.000 claims 1
229910052750 molybdenum Inorganic materials 0.000 claims 1
239000011733 molybdenum Substances 0.000 claims 1
229910021647 smectite Inorganic materials 0.000 claims 1
235000011149 sulphuric acid Nutrition 0.000 claims 1
239000001117 sulphuric acid Substances 0.000 claims 1
125000006617 triphenylamine group Chemical group 0.000 claims 1
238000004519 manufacturing process Methods 0.000 abstract description 5
238000003786 synthesis reaction Methods 0.000 description 75
239000010410 layer Substances 0.000 description 73
238000004458 analytical method Methods 0.000 description 32
238000000434 field desorption mass spectrometry Methods 0.000 description 27
125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 27
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Natural products C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 20
238000000034 method Methods 0.000 description 19
239000007787 solid Substances 0.000 description 19
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 16
125000003277 amino group Chemical group 0.000 description 16
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 14
239000007943 implant Substances 0.000 description 13
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 12
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 11
239000000243 solution Substances 0.000 description 11
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 10
238000006243 chemical reaction Methods 0.000 description 10
DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 10
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 10
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 10
125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 9
241000234282 Allium Species 0.000 description 9
235000002732 Allium cepa var. cepa Nutrition 0.000 description 9
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
239000004305 biphenyl Substances 0.000 description 9
125000004122 cyclic group Chemical group 0.000 description 9
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical class C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
125000004104 aryloxy group Chemical group 0.000 description 8
229910052757 nitrogen Inorganic materials 0.000 description 8
125000005561 phenanthryl group Chemical group 0.000 description 8
239000011347 resin Substances 0.000 description 8
229920005989 resin Polymers 0.000 description 8
229910052707 ruthenium Inorganic materials 0.000 description 8
239000000758 substrate Substances 0.000 description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
235000010290 biphenyl Nutrition 0.000 description 7
BAVYZALUXZFZLV-UHFFFAOYSA-N mono-methylamine Natural products NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 7
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 6
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 6
125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 6
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 6
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 5
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 5
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 5
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
238000009833 condensation Methods 0.000 description 5
230000005494 condensation Effects 0.000 description 5
238000001816 cooling Methods 0.000 description 5
230000000694 effects Effects 0.000 description 5
125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 5
229960005181 morphine Drugs 0.000 description 5
239000012044 organic layer Substances 0.000 description 5
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 5
239000001301 oxygen Substances 0.000 description 5
229910052760 oxygen Inorganic materials 0.000 description 5
YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 4
125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 4
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 4
YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 4
239000002253 acid Substances 0.000 description 4
239000000956 alloy Substances 0.000 description 4
229910045601 alloy Inorganic materials 0.000 description 4
125000005577 anthracene group Chemical group 0.000 description 4
150000001454 anthracenes Chemical class 0.000 description 4
125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 description 4
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
125000006267 biphenyl group Chemical group 0.000 description 4
230000000052 comparative effect Effects 0.000 description 4
229920001577 copolymer Polymers 0.000 description 4
239000012043 crude product Substances 0.000 description 4
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 4
DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 4
230000006870 function Effects 0.000 description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 4
125000004433 nitrogen atom Chemical group N* 0.000 description 4
FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical group CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 4
YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 4
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 4
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 4
238000010898 silica gel chromatography Methods 0.000 description 4
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 4
229910052717 sulfur Inorganic materials 0.000 description 4
125000001544 thienyl group Chemical group 0.000 description 4
VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical group NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 description 3
MKZHJJQCUIZEDE-UHFFFAOYSA-N 1-[(2-hydroxy-3-naphthalen-1-yloxypropyl)-propan-2-ylamino]-3-naphthalen-1-yloxypropan-2-ol Chemical compound C1=CC=C2C(OCC(O)CN(CC(O)COC=3C4=CC=CC=C4C=CC=3)C(C)C)=CC=CC2=C1 MKZHJJQCUIZEDE-UHFFFAOYSA-N 0.000 description 3
YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 3
125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 3
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
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GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 3
239000004793 Polystyrene Substances 0.000 description 3
206010036790 Productive cough Diseases 0.000 description 3
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125000005997 bromomethyl group Chemical group 0.000 description 3
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 3
150000004985 diamines Chemical class 0.000 description 3
238000011156 evaluation Methods 0.000 description 3
229910052731 fluorine Inorganic materials 0.000 description 3
125000001153 fluoro group Chemical group F* 0.000 description 3
229910052733 gallium Inorganic materials 0.000 description 3
125000005842 heteroatom Chemical group 0.000 description 3
125000003707 hexyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 3
150000002429 hydrazines Chemical class 0.000 description 3
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 3
150000002576 ketones Chemical class 0.000 description 3
239000007788 liquid Substances 0.000 description 3
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 3
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 3
229910052763 palladium Inorganic materials 0.000 description 3
RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 3
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 3
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150000004032 porphyrins Chemical class 0.000 description 3
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208000024794 sputum Diseases 0.000 description 3
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239000011593 sulfur Substances 0.000 description 3
150000003573 thiols Chemical group 0.000 description 3
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239000004743 Polypropylene Substances 0.000 description 2
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Classifications

- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
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Optics & Photonics (AREA)
Electroluminescent Light Sources (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
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TW097122736A 2007-06-18 2008-06-18 Aromatic amine derivative and organic electroluminescent element using the same TW200914579A (en)

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US (1)	US20100187511A1 (ja)
EP (1)	EP2159217A4 (ja)
JP (1)	JPWO2008156089A1 (ja)
KR (1)	KR20100017849A (ja)
TW (1)	TW200914579A (ja)
WO (1)	WO2008156089A1 (ja)

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KR100835601B1 (ko)	2007-01-26	2008-06-09	주식회사 두산	비대칭 스티릴 유도체 및 이를 이용한 유기 전계 발광 소자
WO2009066600A1 (ja) *	2007-11-19	2009-05-28	Idemitsu Kosan Co., Ltd.	モノベンゾクリセン誘導体、及びそれを含む有機エレクトロルミネッセンス素子用材料、並びにそれを用いた有機エレクトロルミネッセンス素子
JP5193295B2 (ja)	2008-05-29	2013-05-08	出光興産株式会社	芳香族アミン誘導体及びそれらを用いた有機エレクトロルミネッセンス素子
WO2010016405A1 (ja) *	2008-08-07	2010-02-11	出光興産株式会社	新規芳香族アミン誘導体及びそれを用いた有機エレクトロルミネッセンス素子
KR101178219B1 (ko) *	2008-11-21	2012-08-29	롬엔드하스전자재료코리아유한회사	전기발광화합물을 발광재료로서 채용하고 있는 전기발광소자
JPWO2010122799A1 (ja) *	2009-04-24	2012-10-25	出光興産株式会社	芳香族アミン誘導体及びそれを用いた有機エレクトロルミネッセンス素子
KR20100130059A (ko) *	2009-06-02	2010-12-10	다우어드밴스드디스플레이머티리얼 유한회사	신규한 유기 발광 화합물 및 이를 포함하는 유기 발광 소자
CN102442993A (zh) *	2010-10-12	2012-05-09	中国科学院化学研究所	具有二苯并基团的化合物和它的衍生物、制备它们的方法和它们的用途
TW201226525A (en) *	2010-11-22	2012-07-01	Idemitsu Kosan Co	Organic electroluminescent element
KR101952707B1 (ko)	2012-01-03	2019-06-03	삼성디스플레이 주식회사	신규한 화합물 및 이를 포함한 유기발광 소자
KR101695351B1 (ko)	2012-07-25	2017-01-13	삼성디스플레이 주식회사	축합환 화합물 및 이를 포함하는 유기 전계 발광 소자
KR102428221B1 (ko) *	2017-08-09	2022-08-02	덕산네오룩스 주식회사	유기전기 소자용 화합물, 이를 이용한 유기전기소자 및 그 전자 장치
KR20220029590A (ko) *	2019-07-08	2022-03-08	소니그룹주식회사	화합물, 폴리머 및 유기 재료, 및 이를 사용한 광학 장치, 광학 부품 및 화상 표시 장치

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US48688A (en) *		1865-07-11		Improved carriage-top
DE69333840T2 (de) *	1992-08-28	2005-12-01	Idemitsu Kosan Co. Ltd.	Ladungsinjektionszusatzmaterial
JP3890686B2 (ja) *	1997-07-22	2007-03-07	東洋インキ製造株式会社	有機エレクトロルミネッセンス素子
JP4094203B2 (ja) *	2000-03-30	2008-06-04	出光興産株式会社	有機エレクトロルミネッセンス素子及び有機発光媒体
JP2004087245A (ja) *	2002-08-26	2004-03-18	Fuji Photo Film Co Ltd	発光素子
JP4181399B2 (ja) *	2002-12-19	2008-11-12	三井化学株式会社	ジアミン化合物、および該ジアミン化合物を含有する有機電界発光素子
US7147938B2 (en) *	2004-06-30	2006-12-12	Eastman Kodak Company	Organic element for electroluminescent devices
US7544425B2 (en) *	2004-10-29	2009-06-09	Eastman Kodak Company	Organic element for electroluminescent devices
EP1834946A4 (en) *	2005-01-05	2009-04-29	Idemitsu Kosan Co	AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE USING THIS
CN101268167A (zh) *	2005-09-16	2008-09-17	出光兴产株式会社	芘系衍生物以及应用该衍生物的有机电致发光元件
JP5090639B2 (ja) *	2005-11-18	2012-12-05	出光興産株式会社	芳香族アミン誘導体及びそれを用いた有機エレクトロルミネッセンス素子
KR100835601B1 (ko) *	2007-01-26	2008-06-09	주식회사 두산	비대칭 스티릴 유도체 및 이를 이용한 유기 전계 발광 소자

2008
- 2008-06-17 EP EP08765691.4A patent/EP2159217A4/en not_active Withdrawn
- 2008-06-17 WO PCT/JP2008/061058 patent/WO2008156089A1/ja not_active Ceased
- 2008-06-17 US US12/665,050 patent/US20100187511A1/en not_active Abandoned
- 2008-06-17 KR KR1020097026342A patent/KR20100017849A/ko not_active Ceased
- 2008-06-17 JP JP2009520490A patent/JPWO2008156089A1/ja active Pending
- 2008-06-18 TW TW097122736A patent/TW200914579A/zh unknown

Also Published As

Publication number	Publication date
WO2008156089A1 (ja)	2008-12-24
KR20100017849A (ko)	2010-02-16
EP2159217A1 (en)	2010-03-03
EP2159217A4 (en)	2013-08-28
US20100187511A1 (en)	2010-07-29
JPWO2008156089A1 (ja)	2010-08-26

Publication	Publication Date	Title
TW200914579A (en)	2009-04-01	Aromatic amine derivative and organic electroluminescent element using the same
KR101169901B1 (ko)	2012-07-31	방향족 아민 유도체 및 이를 이용한 유기 전기발광 소자
JP5139297B2 (ja)	2013-02-06	芳香族アミン誘導体及びそれらを用いた有機エレクトロルミネッセンス素子
KR100949214B1 (ko)	2010-03-24	방향족 아민 유도체 및 그것을 사용한 유기 전기발광 소자
KR101213383B1 (ko)	2012-12-17	플루오렌계 유도체 및 이를 이용한 유기 전기발광 소자
TW200916434A (en)	2009-04-16	Aromatic amine derivatives and organic electroluminescent device
TW200932870A (en)	2009-08-01	Aromatic amine derivatives and organic electroluminescence device using the same
TW200902676A (en)	2009-01-16	Organic electroluminescent device
KR20080114784A (ko)	2008-12-31	비스안트라센 유도체 및 그것을 이용한 유기 전기발광 소자
TW201100396A (en)	2011-01-01	Aromatic amine derivative, and organic electroluminescent element comprising same
TW200804232A (en)	2008-01-16	Benzanthracene derivative and electroluminescence device using the same
WO2004018587A1 (ja)	2004-03-04	有機エレクトロルミネッセンス素子及びアントラセン誘導体
TW200831636A (en)	2008-08-01	Material for organic electroluminescent element and organic electroluminescent element employing the same
TW201141990A (en)	2011-12-01	Biscarbazole derivative, material for organic electroluminescence device and organic electroluminescence device using the same
KR20080109850A (ko)	2008-12-17	방향족 아민 유도체 및 그것을 이용한 유기 전기 발광 소자
TW201033330A (en)	2010-09-16	Organic electroluminescent element material and organic electroluminescent element comprising same
TW201016638A (en)	2010-05-01	Anthracene derivative, and organic electroluminescence element comprising same
EP2423179A1 (en)	2012-02-29	Aromatic amine derivative and organic electroluminescent element comprising same
JPWO2010018842A1 (ja)	2012-01-26	ベンゾフルオランテン誘導体及びそれを用いた有機エレクトロルミネッセンス素子
TW200948786A (en)	2009-12-01	Nitrogen-containing heterocyclic derivative and organic electroluminescent device using the same
KR20100116180A (ko)	2010-10-29	방향족 아민 유도체 및 그것을 사용한 유기 전기발광 소자
TW201313681A (zh)	2013-04-01	芳香族胺衍生物及使用其之有機電致發光元件
KR101296029B1 (ko)	2013-08-12	바이페닐 유도체, 유기 전기발광 소자용 재료, 및 그것을이용한 유기 전기발광 소자
TW201033328A (en)	2010-09-16	Organic electroluminescence element and compound
KR101345055B1 (ko)	2013-12-26	방향족 아민 유도체 및 그것을 이용한 유기 전계발광 소자